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RBM10

Official Full Name
RNA binding motif protein 10
Organism
Homo sapiens
GeneID
8241
Background
This gene encodes a nuclear protein that belongs to a family proteins that contain an RNA-binding motif. The encoded protein associates with hnRNP proteins and may be involved in regulating alternative splicing. Defects in this gene are the cause of the X-linked recessive disorder, TARP syndrome. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2011]
Synonyms
S1-1; TARPS; GPATC9; ZRANB5; GPATCH9; DXS8237E; MINAS-60;

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